Canonical Allele Identifier: PA915976121
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 411289
ClinVar RCV Id: RCV000457905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Ser892Gly
CA16615492
NM_001134408.2:c.2674A>G